Dev. Biol. 1999 Apr
Lobe CG, Koop KE, Kreppner W, Lomeli H, Gertsenstein M, Nagy A
Abstract
The Cre/loxP site-specific recombination system combined with embryonic stem cell-mediated technologies has greatly expanded our capability to address normal and disease development in mammals using genetic approaches. The success of this emerging technology hinges on the production of Cre-expressing transgenic lines that provide cell type-, tissue-, or developmental stage-specific recombination between loxP sites placed in the genome. Here we describe and characterize the production of a double
...[more]-reporter mouse line that provides a convenient and reliable readout of Cre recombinase activity. Throughout all embryonic and adult stages, the transgenic animal expresses the lacZ reporter gene before Cre-mediated excision occurs. Cre excision, however, removes the lacZ gene, allowing expression of the second reporter, the human alkaline phosphatase gene. This double-reporter transgenic line is able to indicate the occurrence of Cre excision in an extremely widespread manner from early embryonic to adult lineages. It will be a valuable reagent for the increasing number of investigators taking advantage of the powerful tools provided by the Cre/loxP site-specific recombinase system.
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Mesh Headings:
Alkaline Phosphatase, Animals, Cell Aggregation, Embryo, Mammalian, Gene Expression, Genes, Reporter, Genetic Vectors, Genotype, Histocytochemistry, Integrases, Lac Operon, Mice, Mice, Transgenic, Ploidies, Recombination, Genetic, Sequence Deletion, Stem Cells, Tissue Distribution, Transgenes, Viral Proteins